Variant report

Variant rs227168
Chromosome Location chr1:210256723-210256724
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:210248600-210261000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:210248600-210273200 Weak transcription Fetal Brain Female brain
3 chr1:210250400-210263000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:210250800-210258000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr1:210250800-210260400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr1:210250800-210278800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr1:210251400-210260200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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